Surfaces having particles and related methods

ABSTRACT

Provided are surfaces comprising particles, which particles may possess, for example, antimicrobial or biosensing properties. Also provided are related methods for fabrication of the inventive articles. Also provided are systems and methods for treating fluids, objects, and targets with the inventive surfaces.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No.60/932,025, filed May 29, 2007, and of U.S. Provisional Application61/126,589 filed May 6, 2008, the entireties of which are incorporatedby reference herein.

FIELD OF THE INVENTION

The present invention relates to the fields of active particles and ofpolymer-solvent interactions.

BACKGROUND OF THE INVENTION

Functionalizing surfaces by implantation of active, functional particlesis an area of interest to a number of fields. By functionalizingsurfaces with particles, users may create surfaces that present theuseful properties of the particles, such as antimicrobial properties andbiosensing.

One area where functionalized surfaces is of particular interest is thereduction of microbial contamination. It is estimated that microbialcontamination costs billions of dollars in equipment damage, productcontamination, energy losses, and medical infections each year. As oneexample of the magnitude of this problem, microbial-related damage tobuildings and building materials is estimated at several billions ofdollars each year.

Microbial contamination also causes significant illness and attendantloss of productivity. Commonly used devices such as phones, automaticteller machines (ATMs), and computer keyboards characteristicallypresent microbial densities many times greater than the microbialdensities present on toilet seats and other similar fixtures.

Interest in functional surfaces is not limited to antimicrobialsurfaces. As one example, surfaces having the ability to bind tospecific biological molecules are also of interest.

Plastics also typically contain a variety of additives—such asplasticizers and lubricants—to help achieve certain desired properties.These additives also, however, provide the carbon needed to sustain thegrowth and proliferation of microbes. Hence, while plastics typicallyrequire one or more additives to achieve a particular characteristic,such additive-laden plastics may also be susceptible to microbialcontamination.

At present, substrate-particle composites that include particles ofvarious functionalities are made by two methods. In the common bulkincorporation method of production, particles are non-specificallydispersed throughout the entirety of a substrate. In common coatingprocesses, particles are dispersed within a secondary coating layer thatis then disposed atop the main substrate or even atop additional primeror binder layers.

These methods, however, pose certain disadvantages. Bulk incorporationis inefficient in that while the goal of the method is to produce asubstrate having particles on the surface, a large number of particlesare also dispersed within the substrate. Thus, in bulk incorporation, alarge number of particles are effectively buried within the substrateand can not be presented to the environment exterior to the substrate.As a result, a comparatively large number of particles are needed tofunctionalize the surfaces of a given substrate by way of bulkincorporation. Also, achieving uniform dispersion of particles withinthe substrate is difficult, but may nevertheless be necessary foruniform surface area coverage of the particles.

Coating processes also present certain inefficiencies. Use of a coatingprocess to make a functionalized surface can involve multiple additionalmanufacturing steps, including surface pretreatment, priming, andcuring. Second, the coating layer must sufficiently adhere or bind tothe underlying substrate so as to avoid detachment from the substrate,which is especially challenging for polymer substrates. Proper executionof coating-based techniques may require significant research anddevelopment commitments, and may also require additional primer layersor surface treatments. Third, the coating layer must sufficiently entrapparticles in order to prevent particles from loosening and escapingunder use conditions.

Accordingly, there is a need in the art for composite structures havingsurface-borne particles that are securely and efficiently attached tothe surfaces. The value of such structures would be enhanced if thestructures presented such particles on the surface and the structuresdid not include unnecessary particles within that were not available topresentation to the environment exterior to the structure. There arealso parallel needs for fabricating such structures and for otherrelated devices.

SUMMARY OF THE INVENTION

In meeting the described challenges, the present invention firstprovides methods of embedding particles in a substrate, comprisingapplying to at least a portion of a substrate a fluid comprising apopulation of particles having at least one characteristic dimension inthe range of from about 0.1 nm to about 1 cm, such that the substrate issoftened to at least a degree that a plurality of particles is at leastpartially embedded in the softened portion of the substrate; andhardening at least a portion of the substrate so as to give rise to atleast one particle being securely embedded in the substrate.

The present invention further provides composite materials, thematerials comprising a substrate having at least one surface in which apopulation of particles is at least partially embedded, the populationof particles having an average characteristic dimension in the range offrom about 0.1 nm to about 1 cm.

Also provided are compositions for functionalizing a substrate,comprising a population of particles disposed in a fluid, thecomposition being capable of softening a substrate at least to thedegree that one or more particles is capable of being embedded at leastpartially within the softened polymeric substrate.

In addition, the present invention also provides systems for treating afluid, comprising a structure having at least one surface in which apopulation of functionalized particles is at least partially embedded,the population of particles having an average characteristic dimensionin the range of from about 0.1 nm to about 1 cm; and a supply of fluid.

Further provided is a method of treating targets, comprising contactingone or more targets having one or more components with a surfacecomprising a population of particles partially embedded in the surface,the population of partially embedded particles comprising an averagecharacteristic dimension in the range of from 0.1 nm to about 1 cm, thecontacting being performed so as to give rise to one or more of thepartially embedded particles interacting with one or more components ofthe target.

The present invention also provides methods of embedding particles inpolymeric substrates, comprising applying, to a substrate, a populationof particles to the substrate under such conditions that one or more ofthe particles is at least partially embedded in the substrate, thepopulation of particles comprising an average characteristic dimensionin the range of from about 0.1 nm to about 1 cm.

Additionally provided are methods of distributing particles across asurface, comprising dispersing a population of particles in a fluidinert to at least one substrate; and disposing the fluid across asurface of the at least on substrate.

BRIEF DESCRIPTION OF THE DRAWINGS

The summary, as well as the following detailed description, is furtherunderstood when read in conjunction with the appended drawings. For thepurpose of illustrating the invention, there are shown in the drawingsexemplary embodiments of the invention; however, the invention is notlimited to the specific methods, compositions, and devices disclosed. Inaddition, the drawings are not necessarily drawn to scale. In thedrawings:

FIG. 1 depicts a schematic cross-sectional view of particles that arebulk-dispersed within a material;

FIG. 2 depicts a cross-sectional schematic view of particles that havebeen applied to one side of a substrate by a traditional coating method;

FIG. 3 depicts a cross-sectional schematic view of the claimedmaterials, depicting a population of particles partially embedded withinone side of a substrate material;

FIG. 4 depicts a schematic view of applying an active material to asubstrate according to the claimed invention, using a conventional sprayapplicator method;

FIG. 5 depicts a schematic view of a several active particles embeddedin a substrate according to the present invention;

FIG. 6 illustrates scanning electron micrographs of (a) E. coli cells(a) and (b) cells treated with 50 μg/cm³ silver nanoparticles in liquid;

FIG. 7 illustrates optical micrographs of a hot-pressed flat PVC samplehaving aerosol-delivered silver nanoparticles (right-hand image) and acontrol sample without silver (left-hand image);

FIG. 8 illustrates Raman scattering associated with silver nanoparticlesand the silver-enhanced and plain PVC samples;

FIG. 9 illustrates optical micrographs of PVC samples treated withsilver containing tetrahydrofuran (THF) solutions containing varyingconcentrations of PVC but constant silver concentration (1.5 wt %) at20× magnification;

FIG. 10 illustrates the coated area fraction with increasing silverconcentration for various constant PVC concentrations;

FIG. 11 illustrates an increasing trend in average particle size withincreasing silver concentration at constant PVC concentration;

FIG. 12 illustrates SEM micrographs of a trench cut into un-treated PVC(left) and silver-treated PVC (right) exposing a cross-sectional view ofan embedded silver particle;

FIG. 13 illustrates the area fraction of silver coverage over time forPVC samples enhanced with a 2 wt % silver and 2.25 wt % PVC in THFsolution subject to a water flow rate of 3.9 gal/min·in²;

FIG. 14 illustrates (A) 100 mm Liria-Bertani (LB broth) plates 24 hoursafter inoculation with E. coli. Control (left plate) and withaerosolized Ag nanoparticles (right plate), with red dotted circleshowing target of the air stream, (B) expanded view of bacteria growthboundary regions in FIG. 14A, with a dotted circle showing the target ofthe air stream;

FIG. 15 illustrates (A) an untreated control sample (top, labeled with a“C”) and a sample treated with 2 wt % Ag, 2.25 wt % PVC in THF (bottom)as viewed from underside of agar 24 hours following inoculation with E.coli, and (B) an expanded view of the treated sample from (A), witharrows pointing to zone of inhibition maxima (˜0.88 mm);

FIG. 16 illustrates an untreated control sample (left-most sample), asample treated with 2 wt % Ag, 2.25 wt % PVC, THF solution (second fromleft), a sample treated with 4 wt % Ag, 2.25 wt % PVC, THF solution(third from left), and sterile LB broth (right) after 10 hours. Eachtest tube containing a sample contained LB broth inoculated withequivalent concentration of E. coli, and the decreased turbidity of thebroth containing more heavily treated samples indicates inhibition of E.coli bacterial growth;

FIG. 17 illustrates percentage bacteria coverage of LB agar platesversus time for E. coli-inolculated LB broth in contact with a 4.0 wt %Ag and 2.0 wt % PVC sample and then spread plated;

FIG. 18 illustrates (A) growth of E. coli on untreated control sampleafter 24 hours (left), and reduction of growth of E. coli on a sampletreated with 4 wt % Ag, 2.25 wt % PVC, THF solution (right), and (B)growth of S. aureus on untreated control sample after 24 hours (left),and reduction of growth of S. aureus on a sample treated with 4 wt % Ag,2.25 wt % PVC, THF solution (right);

FIG. 19 illustrates SEM micrographs of a PVC surface treated withtetrahydrofuran containing hexadecylamine-capped silver nanoparticlesembedded into the surface (left) and a surface (right) exposing across-sectional view in the foreground showing the particles embeddeddeep into the surface;

FIG. 20 illustrates optical micrographs of a polycarbonate surfacetreated with a 50/50 mix by volume of 2-methyltetrahydrofuran/acetonecontaining 0.1 wt % Type A zeolite loaded with ionic silver and showingthe zeolite crystal particles embedded into the surface (upper image)and a polycarbonate surface (lower image) treated with a 50/50 mix byvolume of 2-methyltetrahydrofuran/acetone containing 0.1 wt % zirconiumphosphate-based ceramic ion-exchange resin loaded with ionic silver andshowing the resin particles embedded into the surface;

FIG. 21 illustrates SEM micrographs of a polycarbonate surface treatedwith 2-methyltetrahydrofuran containing 0.1 wt % glass microparticlesloaded with ionic silver and showing the particles embedded into thesurface; and

FIG. 22 illustrates (upper left) an optical micrograph of a PVC surfacetreated with 2-methyltetrahydrofuran containing 0.1 wt % carbonnanofiber, showing nanofibers partially embedded into the surface, and(upper right, lower left, and lower right) SEM micrographs showing thenanofibers partially embedded into the surface.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

The present invention may be understood more readily by reference to thefollowing detailed description taken in connection with the accompanyingfigures and examples, which form a part of this disclosure. It is to beunderstood that this invention is not limited to the specific devices,methods, applications, conditions or parameters described and/or shownherein, and that the terminology used herein is for the purpose ofdescribing particular embodiments by way of example only and is notintended to be limiting of the claimed invention. Also, as used in thespecification including the appended claims, the singular forms “a,”“an,” and “the” include the plural, and reference to a particularnumerical value includes at least that particular value, unless thecontext clearly dictates otherwise. The term “plurality”, as usedherein, means more than one. When a range of values is expressed,another embodiment includes from the one particular value and/or to theother particular value. Similarly, when values are expressed asapproximations, by use of the antecedent “about,” it will be understoodthat the particular value forms another embodiment. All ranges areinclusive and combinable.

It is to be appreciated that certain features of the invention whichare, for clarity, described herein in the context of separateembodiments, may also be provided in combination in a single embodiment.Conversely, various features of the invention that are, for brevity,described in the context of a single embodiment, may also be providedseparately or in any subcombination. Further, reference to values statedin ranges include each and every value within that range.

In a first aspect, the present invention provides methods of embeddingparticles in substrates. The claimed methods suitably include applyingto at least a portion of a substrate a fluid comprising a population ofparticles having at least one characteristic dimension in the range offrom about 0.1 nm to about 1 cm.

Application of the fluid is suitably performed to give rise to thesubstrate softening to at least a degree that a plurality of particlesis at least partially embedded in the softened portion of the substrate,which softening may be accomplished solely by the fluid in someembodiments.

The embedding of particles is then suitably followed by hardening atleast a portion of the substrate. The hardening gives rise to at leastone particle being securely embedded in the substrate, as shown in,e.g., FIG. 3 and FIG. 5.

In some embodiments, the population of particles is disposed into thefluid. Disposition may be accomplished by mixing, sonicating, shaking,vibrating, flowing, chemically modifying the particles' surfaces,chemically modifying the fluid, or otherwise motivating or modifying theparticles to achieve the desired dispersion. Other methods for achievingparticle dispersion in a fluid will be known to those of ordinary skillin the art. The dispersion may be uniform or non-uniform.

The fluid in which the particles reside is suitably a gas or a liquid,and is preferably capable of softening the substrate. The fluid is alsosuitably inert to the population of particles and does not alter thechemical or other properties of the particles, and the fluid alsosuitably has little to no effect on the chemical properties of thesubstrate aside from softening the substrate.

In some embodiments—depending on the needs and constraints of theuser—the fluid alters or affects one or more properties of thesubstrate. For example, the fluid may be chosen for its ability to addfunctional groups to the substrate or to neutralize functional groupsthat may be present on the substrate.

Fluids and solvents are, as previously mentioned, suitably chosen on thebasis of their ability to soften a particular substrate in a way that isamenable to a user's needs. For example, while a given solvent may becapable of slowly softening a particular substrate, other solvents maybe more optimal for a user seeking to quickly soften a substrate forhigh-speed incorporation of particles into that particular substrate.The effect of the fluid on the substrate may include solely softeningthe substrate, or may, in some embodiments, also include removal ordissolution of at least a portion of the substrate.

Suitable fluids include—but are not limited to—water, aqueous solutions,organic solvents, inorganic solvents, ionic solutions, solutionscomprising salts, and the like. Fluids may be applied under ambientconditions, but may also be applied under heating, cooling, increased orreduced pressure, vibration, sonication, increased or decreasedhumidity, and the like. The optimal application conditions will beapparent to those of ordinary skill in the art.

Suitable organic solvents include non-polar solvents, polar aproticsolvents, polar protic solvents, and the like. Non-polar solventsinclude hexane, benzene, toluene, diethyl ether, chloroform, ethylacetate, and the like—those of ordinary skill in the art will be awareof other non-polar solvents suitable for use in the claimed invention.

Polar aprotic solvents include 1,4-dioxane, tetrahydrofuran,dichloromethane, acetone, acetonitrile, dimethylformamide, dimethylsulfoxide, and the like. Polar protic solvents include acetic acid,n-butanol, isopropanol, n-propanol, ethanol, methanol, formic acid, andother similar compounds and solutions.

A non-exclusive listing of other, suitable organic solvents includesmethyl ethyl keytone, hexafluoroisopropanol, 1-butanol, 2-butanol,2-butanone, t-butyl alcohol, carbon tetrachloride, chloro benzene,cyclohexane, 1,2-dichloro ethane, diethyl ether, diethylene glycol,diglyme, 1,2-dimethoxyethane, dimethylether, dioxane, ethyl acetate,ethylene glycol, glycerine, heptane, hexamethylphosphoramide,hexamethylphosphorous triamide, methyl t-butyl ether, methylenechloride, N-methyl-2-pyrrolidinone, nitromethane, pentane, petroleumether, 1-propanol, 2-propanol, pyridine, triethyl amine, o-xylene,m-xylene, p-xylene, trifluoroethanol, diethyl ether, carbon disulfide,mineral oil,

isopropylamine, aniline, cycloaliphatic hydrocarbons,tetrahydronaphthalene, tetrachloroethane, tetrafluoropropanol, afluoro-hydrocarbon, a chloro-hydrocarbon, methyl acetate, methylformate, a ketone, 2-methyltetrahydrofuran, cyclopentyl methyl ether,methyl n-propyl ketone, a paraffin, an olefin, an alkyne, and othersimilar compounds or solutions. Alcohols and acids may also be suitablefluids, depending on the substrate and particles being used.

Inorganic solvents suitable for the claimed invention include ammonia,sulfur dioxide, sulfuryl chloride, sulfuryl chloride fluoride,phosphoryl chloride, and phosphorus tribromide. Dinitrogen tetroxide,antimony trichloride, bromine pentafluoride, and hydrogen fluoride arealso considered useful.

A variety of ionic solutions are used in the claimed invention. Thesesolutions include choline chloride, urea, malonic acid, phenol,glycerol, 1-alkyl-3-methylimidazolium, 1-alkylpyridinium,N-methyl-N-alkylpyrrolidinium, 1-Butyl-3-methylimidazoliumhexafluorophosphate, ammonium, choline, imidazolium, phosphonium,pyrazolium, pyridinium, pyrrolidinium, sulfonium,1-ethyl-1-methylpiperidinium methyl carbonate, and4-ethyl-4-methylmorpholinium methyl carbonate.

Other methylimidazolium solutions are considered suitable, including1-Ethyl-3-methylimidazolium acetate, 1-butyl-3-methylimidazoliumtetrafluoroborate, 1-n-butyl-3-methylimidazolium tetrafluoroborate,1-butyl-3-methylimidazolium hexafluorophosphate,1-n-butyl-3-methylimidazolium hexafluorophosphate,1-butyl-3-methylimidazolium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide,1-butyl-3-methylimidazolium bis[(trifluoromethyesulfonyl)]amide, and1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide.

Halogenated compounds are also suitable. These compounds includeN-ethyl-N,N-bis(1-methylethyl)-1-heptanaminiumbis[(trifluoromethyl)sulfonyl]imide,ethylheptyl-di-(1-methylethyl)ammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,ethylheptyl-di-(1-methylethyl)ammoniumbis(trifluoromethylsulfonyl)imide,ethylheptyl-di-(1-methylethyl)ammoniumbis[(trifluoromethyl)sulfonyl]amide.

Imides and amides are also properly included in the claimed invention. Anon-exclusive listing of these compounds includesethylheptyl-di-(1-methylethyl)ammoniumbis[(trifluoromethyl)sulfonyl]imide, N,N,N-tributyl-1-octanaminiumtrifluoromethanesulfonate; tributyloctylammonium triflate,tributyloctylammonium trifluoromethanesulfonate,N,N,N-tributyl-1-hexanaminium bis[(trifluoromethyl)sulfonyl]imide,tributylhexylammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,tributylhexylammonium bis(trifluoromethylsulfonyl)imide,tributylhexylammonium bis[(trifluoromethyl)sulfonyl]amide,tributylhexylammonium bis[(trifluoromethyl)sulfonyl]imide,N,N,N-tributyl-1-heptanaminium bis[(trifluoromethyl)sulfonyl]imide,tributylheptylammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methane sulfonamide,tributylheptylammonium bis(trifluoromethylsulfonyl)imide;tributylheptylammonium bis[(trifluoromethyl)sulfonyl]amide,tributylheptylammonium bis[(trifluoromethyl)sulfonyl]imide,N,N,N-tributyl-1-octanaminium bis[(trifluoromethyl)sulfonyl]imide,tributyloctylammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,tributyloctylammonium bis(trifluoromethylsulfonyl)imide,tributyloctylammonium bis[(trifluoromethyl)sulfonyl]amide,tributyloctylammonium bis[(trifluoromethyl)sulfonyl]imide,1-butyl-3-methylimidazolium trifluoroacetate,1-methyl-1-propylpyrrolidinium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,1-methyl-1-propylpyrrolidinium bis(trifluoromethylsulfonyl)imide,1-methyl-1-propylpyrrolidinium bis[(trifluoromethyl)sulfonyl]amide,1-methyl-1-propylpyrrolidinium bis[(trifluoromethyl)sulfonyl]imide,1-butyl-1-methylpyrrolidinium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide,1-butyl-1-methylpyrrolidinium bis[(trifluoromethyl)sulfonyl]amide,1-butyl-1-methylpyrrolidinium bis[(trifluoromethyl)sulfonyl]imide,1-butylpyridinium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,1-butylpyridinium bis(trifluoromethylsulfonyl)imide, 1-butylpyridiniumbis[(trifluoromethyl)sulfonyl]amide, 1-butylpyridiniumbis[(trifluoromethyl)sulfonyl]imide, 1-butyl-3-methylimidazoliumbis(perfluoroethylsulfonyl)imide, butyltrimethylammoniumbis(trifluoromethylsulfonyl)imide, 1-octyl-3-methylimidazolium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,1-octyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide,1-octyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]amide,1-octyl-3-methylimidazolium bis[(thfluoromethyl)sulfonyl]imide,1-ethyl-3-methylimidazolium tetrafluoroborate,N,N,N-trimethyl-1-hexanaminium bis[(trifluoromethyl)sulfonyl]imide;hexyltrimethylammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,hexyltrimethylammonium bis(trifluoromethylsulfonyl)imide,hexyltrimethylammonium bis[(trifluoromethyl)sulfonyl]amide,hexyltrimethylammonium bis[(trifluoromethyl)sulfonyl]imide,N,N,N-trimethyl-1-heptanaminium bis[(trifluoromethyl)sulfonyl]imide,heptyltrimethylammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,heptyltrimethylammonium bis(trifluoromethylsulfonyl)imide,heptyltrimethylammonium bis[(trifluoromethyl)sulfonyl]amide,heptyltrimethylammonium bis[(trifluoromethyl)sulfonyl]imide,N,N,N-trimethyl-1-octanaminium bis[(trifluoromethyl)sulfonyl]imide,trimethyloctylammonium1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide,trimethyloctylammonium bis(trifluoromethylsulfonyl)imide,trimethyloctylammonium bis[(trifluoromethyl)sulfonyl]amide,trimethyloctylammonium bis[(trifluoromethyl)sulfonyl]imide,1-ethyl-3-methylimidazolium ethyl sulfate, and the like.

As will be apparent to those of skill in the art, a variety of solventsare useful, and those of ordinary skill in the art will encounter littledifficulty in determining the optimal solvent for use in a givenapplication. Solvents may be chosen based on their compatibility with aparticular substrate-particles combination. Alternatively, solvents maybe chosen based on their volatility, the classification by governingbodies, or economic constraints of the user.

The fluid may also include salts, surfactants, stabilizers, and otheradditives that may be useful in conferring a particular property on thefluid. Stabilizers are typically chosen based on their ability to atleast partially inhibit inter-particle agglomeration. Other stabilizersmay be chosen based on their ability to preserve the functionality of aparticle while that particle is being stored or is being incorporatedinto a substrate according to the claimed methods. Other additives maybe used to adjust the fluid's rheological properties, evaporation rate,and other properties.

The fluid may be applied such that it is stationary relative to thesubstrate. In these embodiments, the fluid is disposed atop thesubstrate for a period of time. In other embodiments, at least one ofthe substrate and fluid moves relative to the another—as examples, thefluid may be sprayed on to the substrate, or the substrate may beconveyed through a falling curtain of fluid or conveyed through a poolor bath of fluid. Fluid can also be sprayed, spin cast, dipped, paintedon, brushed on, immersed, and the like.

An exemplary view of the claimed methods is shown in FIG. 4, whichfigure depicts the application of fluid-borne particles to a substratevia a standard painting or coating apparatus. Because the fluid-borneparticles may be applied by various means, little to no adaptation ofexisting application equipment is necessary to perform the claimedmethods. The partial embedding of the particles is shown schematicallyin FIG. 5. The optimal method of applying the fluid to the substratewill be dictated by the needs of the user and will be apparent to thoseof ordinary skill in the art. In some embodiments, essentially all theparticles present in a given finished article are present on the surfaceof the article, as distinction from the bulk-incorporation articlesdescribed elsewhere herein.

Application may be effected by spraying, painting, spin casting,dripping, dipping, dripping, painting, brushing, immersing and the like.In some embodiments, a gradient is applied to the fluid, particles, orboth. Suitable gradients include magnetic and electric fields. Thegradient may be used to apply or disperse the fluid, particles, or both,to the substrate. In some embodiments, the gradient is used tomanipulate one or more particles so as to more deeply embed or drive theone or more particles into the substrate. In other embodiments, thegradient is used to remove or de-embed particles from the substrate.

An applied gradient be constant or variable as dictated by the user'sneeds. Gradients may be applied before the substrate is softened, whilethe substrate is softened, or even after the substrate is softened. Thestrength and orientation of a suitable gradient will be apparent tothose of ordinary skill in the art.

The population of particles is suitably essentially uniformly dispersedwithin the fluid, although non-homogeneous dispersions of particles arewithin the scope of the present invention. Particles may also beagglomerated, depending on the needs of the user.

The methods also suitably include heating the substrate to at leastpartially soften at least a portion of the substrate, heating the fluid,heating one or more particles, or any combination thereof. Depending onthe particles and substrate involved, application of heat may enhancethe embedding of the particles into the substrate.

Particles suitable for the present methods are described in additionaldetail elsewhere herein, and suitably include one or more functionalagents. Functional agents include antimicrobial agents, biocidal agents,insulators, conductors, semiconductors, catalysts, fluorescent agents,flavor agents, catalysts, ligands, receptors, antibodies, nucleic acids,antigens, labels or tags—which may be radioactive or magnetic,lubricants, fragrances, and the like. As an example, a particle mayinclude silver or silver ions, which are known to have antimicrobialproperties. Other functionalized particles are described elsewhereherein in additional detail.

The particle population applied to the substrate may include two or moreparticles of different sizes, of different compositions, or evenparticles of different sizes and different compositions. For example, auser may require a surface that has biocidal properties and possesses apleasing fragrance. In such a case, the user may utilize biocidal silverparticles of one size and fragrant particles of another size.

The particle population may be mono- or polydisperse, depending on theneeds of the user and the user's access to particulate materials. Theneeds of the user will also dictate the composition and distribution ofparticles used in a given application. In some cases, the monodispersityof the particles embedded in the substrate may be of little to noimportance. In other cases, such as where the functionality of theparticle-substrate composition depends at least in part on on particlesize, monodispersity may have increased importance.

One or more particles may be harder than the substrate prior to thesubstrate's softening. In alternative embodiments, substrate may also beharder than the particles.

Suitable substrates include polymers, rubbers, woods, and the like. Theclaimed methods are generally applicable to any material that is capableof being reversibly softened.

Suitable substrates are described in additional detail elsewhere hereinand include single polymers or multiple polymers. The claimed methodsmay also be applied to existing coatings disposed on substrates; forexample, the claimed methods are applicable to paints, insulators, andother coatings. Polyvinyl chloride (PVC) is considered an especiallysuitable for the present invention. Application of the claimed inventionto a PVC substrate is described in additional detail elsewhere herein.Polypropylene, polycarbonate, and other common plastics used in consumerand industrial applications are also considered especially suitable.

Wood materials suitable for the claimed methods include hardwood,softwood, plywood, particleboard, fiberboard, and the like. The claimedmethods are also suitable for polymer-wood composite materials andengineered wood products.

Following softening of the substrate, the substrate may be hardened byexposure to ambient conditions. In some embodiments, the substrate ishardened by cooling the substrate. In other embodiments, the substrateis hardened by evaporating at least a portion of the fluid, applyingairflow to the substrate, applying a vacuum to the substrate, and thelike. Combinations of methods for hardening a substrate are alsosuitable. Other methods for hastening the hardening of the substratewill be apparent to those of ordinary skill in the art.

In some embodiments, the methods result in the particles that aresecurably embedded in the substrate being distributed essentiallyuniformly across the substrate. In other cases, the partially embeddedparticles achieve a non-uniform distribution.

The present invention also includes substrates having particles embeddedtherein according to the claimed methods.

In another aspect, the present invention provides composite materials.These materials include a substrate having at least one surface in whicha population of particles is at least partially embedded, with thepopulation of particles having an average characteristic dimension inthe range of from about 0.1 nm to about 1 cm.

Particles may also have characteristic dimensions of from about 1 nm toabout 500 nm, or from about 10 nm to about 100 nm, or even in the rangeof from about 20 nm to about 50 nm. As discussed elsewhere herein,particles may be spherical in shape, but spherical shaped-particles arenot necessary to the invention and the invention is not limited to suchparticles. As non-limiting examples, nanowires and nanotubes—which mayhave diameters of from 1 to 3 nm and lengths in the multiple-micronrange—are suitably used in the claimed invention.

The particles are suitably partially embedded in the substrate, as shownin cross-section in FIG. 3 and also in FIG. 5. FIG. 3 shows in across-sectional view of a structure made according to the claimedinvention, particles partially embedded in the surface of the substrateinstead of being bulk-incorporated throughout the substrate, as shown inFIG. 1 or being present in a separate coating layer that lies atop asubstrate, as shown in FIG. 2. The degree to which a given particle isembedded in the substrate will be a function of a variety of processconditions; those of ordinary skill in the art will appreciatesituations where the degree of embedding may be controlled.

Another example of the disclosed compositions is shown in FIG. 19. Thatfigure shows SEM micrographs of a PVC surface treated withtetrahydrofuran containing hexadecylamine-capped silver nanoparticlesembedded into the surface (left-hand image) and a surface (right-handimage) exposing a cross-sectional view in the foreground showing theparticles embedded deep into the surface.

FIG. 20 illustrates another non-limiting embodiment of the claimedinvention. That figure shows optical micrographs of a polycarbonate (PC)surface treated with a 50/50 mix by volume of2-methyltetrahydrofuran/acetone containing 0.1 wt % Type A zeoliteloaded with ionic silver. The upper image in FIG. 20 shows the zeolitecrystal particles embedded into the surface. The lower image of FIG. 20depicts the polycarbonate surface treated with a 50/50 mix by volume of2-methyltetrahydrofuran/acetone containing 0.1 wt % zirconiumphosphate-based ceramic ion-exchange resin loaded with ionic silver,showing the resin particles embedded into the surface.

FIG. 21 shows another exemplary, non-limiting embodiment of the claimedinvention. In that figure are shown SEM micrographs of a polycarbonatesurface treated with 2-methyltetrahydrofuran containing 0.1 wt % glassmicroparticles loaded with ionic silver, as is apparent, the particlesare securely embedded into the surface.

FIG. 22 illustrates another, alternative embodiment of the claimedinvention, which embodiment demonstrates the applicability of theclaimed invention to nanofibers. In that figure are shown an opticalmicrograph (upper left image) of a PVC surface treated with2-methyltetrahydrofuran containing 0.1 wt % carbon nanofibers, and(upper right, lower left, and lower right) SEM micrographs showingnanofibers partially embedded into the PVC surface.

Suitable substrates include woods, rubbers, polymers, and othermaterials. Homopolymers, copolymers, random polymers, graft polymers,alternating polymers, block polymers, branch polymers, aborescentpolymers, dendritic polymers, and the like are all suitable for use inthe claimed composite materials. Polymers classified as thermoplastics,thermosets, or elastomers are all suitable substrates for the claimedmaterials. Conductive polymers are also considered suitable substrates.

Specifically suitable polymers include polyethylene, polypropylene,polyarylate, polyester, polysulphone, polyamide, polyurethane,polyvinvyl, fluoropolymer, polycarbonate, polylactic acid, nitrile,acrylonitrile butadiene styrene, phenoxy, phenylene ether/oxide, aplastisol, an organosol, a plastarch material, a polyacetal, aromaticpolyamide, polyamide-imide, polyarylether, polyetherimide,polyarylsulfone, polybutylene, polycarbonate, polyketone,polymethylpentene, polyphenylene, polystyrene, styrene maleic anhydride,polyllyl diglycol carbonate monomer, bismaleimide, polyallyl phthalate,epoxy, melamine, silicone, urea, and the like. Other suitable polymerswill be known to those of ordinary skill in the art; cellulosic polymersand other cellulose-based materials are also considered suitable.

Various woods are also suitable for use as substrates in the claimedinvention, including hardwood, softwood, plywood, particleboard,fiberboard, chipboard, flakeboard, strandboard, waferboard, and thelike. Mahogany, walnut, oak, maple, cherry, rosewod, teak, ash, balsa,basswood, beech, cherry, aspen, birch, buckeye, chestnut, cottonwood,dogwood, elm, hackberry, hickory, holly, locust, magnolia, poplar,alder, redbud, royal paulownia, sassafras, sweetgum, sycamore, tupelo,willow, pine, hemlock, fir, redwood, spruce, cedar, larch, redwood, andother woods are all considered suitable.

The substrate may be solid or porous. In the case of a porous substrate,the composite material, in some embodiments, includes particles disposedon the interior walls of the pores. Such porous composite materials arecapable of presenting a comparatively higher surface area—and attendantnumber of embedded particles—to the surrounding environment than solidsubstrate.

The optimal choice of particle for a given composite material willdepend on the needs of the user. Suitable particles include metals,metal oxides, minerals, ceramics, zeolites, polymers, copolymers, andthe like. Silver nanoparticles—having a cross sectional dimension ofless than about 100 nm—and silver-based ceramics are consideredespecially suitable for use in the claimed invention.

Particles suitable for the present invention include one or morefunctionalizing agents. The material of a particle may itself befunctional, or the particle may include one incorporated into or onto aparticle, or both. As will be apparent to those of skill in the art, asingle particle may present multiple functionalities.

Functionalizing agents suitably include antimicrobial agents, biocidalagents, insulators, conductors, semiconductors, catalysts, UV absorbers,fluorescent agents, flavor agents, catalysts, ligands, receptors,antibodies, antigens, labels, lubricants, and the like. The materialfrom which a particle is made may itself be functional. This isexemplified by silver nanoparticles, which are themselves inherentlyantimicrobial.

As another non-limiting example, a polymeric particle may includemultiple ligands bound to its surface so as to enable specific bindingbetween that particle and a particular target. As another non-limitingexample, a silver particle—having biocidal properties—might also includea fragrant agent so as to impart a pleasing smell to a compositematerial that has biocidal properties.

As described elsewhere herein, the particles of the composite materialsmay include particles of the same size or different sizes. The particlesmay also be of the same or different compositions, and may be mono- orpolydisperse. Depending on the user's needs, it may be advantageous tofabricate a composite material that includes several different particleshaving different functionalized agents so as to provide an articlehaving multiple functionalities.

Both the particles, the substrate, or both, may be porous. Particlesaccording to the present invention may be spherical in shape, but mayalso be of different shapes. Cylindrical, tubular, cubic, oblong,spheroid, box-shaped, pyramidal, and randomly-shaped particles are allconsiderer suitable particles shapes. Crystalline shapes—such astetragons, trigons, hexagons, and the like, are also suitable shapes forparticles used in the present invention.

Certain particle types are considered especially suitable for theclaimed materials. As discussed, silver and silver-containing particlesare considered suitable because of their biocidal properties. Otherspecific, suitable particles include carbon nanotubes, carbonnanofibers, carbon nanorods, nanowires, buckyballs, nanoshells,liposomes, dendrimers, quantum dots, magnetic nanoparticles, chlorinatedrubber particles, glasses, polystyrene microparticles,polymethylmethacrylate particles, melamine microparticles, dextrannanoparticles, melamine-formaldehyde particles, latex particles, divinylbenzene carboxyl particles, divinyl benzene carboxyl sulfate particles,polyvinyltoluene particles, shell-layer particles, copper pyrithiones,radioactive particles, shells, and the like.

Particles may also be chosen based on their inherent properties or othercharacteristics. These properties include, inter alia, fragrance,flavor, biosensing, ability to bind to biomolecules, color, reflectance,reactivity, catalytic activity, conductive properties, adsorptiveproperties, insulating properties, semiconducting properties,radioactive properties, antistatic properties, lubricating properties,hydrophobic or hydrophilic properties, and the ability to release one ormore agents into the particle's environment.

In some embodiments, essentially all of the substrate's surface isoccupied by particles. In other embodiments, 75% or more of the at leastone surface is covered by particles, or 50% or more, or 5% or more. Inother embodiments, 10%, 1%, or even less of the surface area is coveredby particles. The optimal particle coverage will be dictated by theneeds of the user—certain composite materials are capable of meeting theuser's needs at a surface coverage of only 1% to 10%, as describedelsewhere herein.

As described elsewhere herein, two or more of the particles may beagglomerated or otherwise adjacent to one another. Clusters of particlesare also suitable in some embodiments.

Separate particles may be separated by distances of from about 0.1 nm toabout 1 mm Particles may be separated by uniform or non-uniformdistances depending on the needs of the user and the method in which thecomposite material was formed. In some embodiments, two or moreparticles are in contact with one another.

Substrates are suitably flat, but may also be cylindrical, polyhedral,spherical, grooved, curved, arced, pitted, hollowed, and the like. Thesubstrate may be in the form of a mesh or filter or other configurationsuitable for contacting a flowing fluid while also permitting passage ofthat fluid.

Substrates are suitably in the range of at least about 0.005 mm inthickness, although thicker and thinner substrates are within the scopeof the present invention. Preferably, the substrate thickness is chosensuch that softening of the substrate or embedding of the particles doesnot compromise the integrity of the substrate or impair the functioningof the final, particle-bearing substrate when placed into use.

One or more particles may be selected based on being harder than thesubstrate. In other embodiments, the substrate is harder than one ormore of the particles. In some applications—such as those where thecomposition may be in physical contact with a moving surface—it may beadvantageous to include comparatively hard particles. In other cases,where mechanical removal of particle material is desired, it ispreferable to utilize comparatively soft particles.

Substrates are suitably chosen to be inert to the embedded particles. Insome cases, the substrate is capable of reaction with one or moreparticles. As one example, a controlled release material may be madewherein the particle-substrate combination is chosen on the basis thatthe substrate will degrade the particles—or vice versa—over time so asto effect release of an agent or the material of the particles overtime. The optimal combinations of substrates and particles will beapparent to those of skill in the art.

it is envisioned that a composite material made according to the claimedmethods is used as a purifier, a sanitizer, a biocide, a detector, alabeler, a filter, a treatment system, or any combination thereof.Several of these applications are discussed in additional detailelsewhere herein.

The present invention also provides compositions for functionalizing asubstrate. These compositions include a population of particles disposedin a fluid, where the composition is capable of softening a substrate atleast to the degree that one or more particles is capable of beingembedded at least partially within the softened polymeric substrate.

Suitable particles and fluids are described elsewhere herein. Thecomposition is useful for functionalizing a variety of substrates, asdescribed elsewhere herein. It is envisioned that the claimedcompositions are particularly useful for functionalizing existingsubstrates, thus enabling modification of legacy systems. As an example,the claimed compositions may be applied to an existing water containmentsystem so as to introduce biocidal particles to the fluid-contactingsurfaces of that system, effectively conferring a sanitizing capabilityon an existing system.

Fluids suitable for the claimed compositions are chosen on the basis oftheir capability of softening a substrate at least to the degree thatone or more particles embeds at least partially within the softenedsubstrate, including when subjected to greater than atmosphericpressure. Fluids may also be suitably selected on the basis of theircapability of softening a polymeric substrate at least to the degreethat one or more particles embeds at least partially within the softenedpolymeric substrate when the one or more particles are propelled againstthe softened polymeric substrate.

The present application also provides systems for treating fluids. Thesesystems suitably include a structure having at least one surface inwhich a population of functionalized particles is at least partiallyembedded, the population of particles having an average characteristicdimension in the range of from about 0.1 nm to about 1 mm; and a supplyof fluid.

The structures of the systems suitably include substrates and particles,as described elsewhere herein. The structures are configured so as toplace a surface comprising one or more partially embedded particles intocontact with the fluid in order to afford the particles the opportunityto interact with the fluid. A suitable structure may be a tube, a pipe,a conduit, a container, a sphere, a trough, a mixer, a baffle, a fin, anagitator, a mesh, a screen, a filter, a membrane, a bottle, a barrel, atank, a channel, and the like. Such structures may be free-standing, asin the case of a pipe. In other cases, the structure is integrated intoa device, such as a groove or conduit that is integrated into ananalysis or diagnostic device.

Structures may be chosen, constructed, or placed singly or multiply soas to maximize fluid-particle contact. As one example, a series offilter-type structures—having the same or different active particles—maybe arrayed so as to provide a multi-stage fluid treatment system.

As one example, the structure may be a particle-treated tube throughwhich fluid passes and reacts with the embedded particles.Alternatively, the structure may be a particle-bearing body that isplaced in a fluid container and then shaken so as to place the particlesinto contact with the fluid. Alternatively, the structure may be aparticle-bearing bristled body through which fluid is passed.

The systems may also include inlets, outlets, and other fluid passages.A system may also include reservoirs or holding tanks to containuntreated fluids, treated fluids, or both. The structures may includeone or more pores if desired; such pores may permit the structure topresent increased surface area to fluids with which the structure iscontacted. The systems may also include pumps, bellows, and otherdevices used to actuate fluid flow.

The described systems are suitably used to purify a fluid, decontaminatea fluid, filter a fluid, label, identify, or otherwise react withcomponents within a fluid, and other like applications. Non-limitingexamples of these are given elsewhere herein. The systems may beportable or stationary.

The claimed invention also discloses methods for treating targets. Thesetreatment methods include contacting one or more targets having one ormore components with a surface comprising a population of particlespartially embedded in the surface, where the population of partiallyembedded particles has an average characteristic dimension in the rangeof from 0.1 nm to about 1 cm. The contacting is then performed so as togive rise to one or more of the partially embedded particles interactingwith one or more components of the target.

Surfaces and particles suitable for use in the claimed treatment methodsare described elsewhere. Targets include fluids, solids, gels,biological materials, and the like. For example, a particle-bearingsurface may be contacted to a solid—such as a doorknob, a keyboard, or atabletop. Alternatively, the particle-bearing solid may be contacted toa fluid—such as a water sample or a blood sample.

The contacting is typically accomplished by touching the surface to thetarget. The target may also be flowed, sprayed, dripped, atomized,overlaid, impressed, nebulized, or otherwise disposed over the surfaceto achieve contact. Particles may occupy essentially all of the surfacearea of a surface. In other embodiments, particles may occupy 75% orless of the surface area of the surface, or less than about 50% of thesurface area, or less than 10% of the surface area. In some embodiments,surfaces that are 5% or 1% covered by particles are suitable for use inthe claimed invention.

Interaction between the particles and the target suitably includespurifying, labeling, disrupting, lysing, binding, chelating, sensing,binding, detecting, and the like. As one illustrative example, a surfacebearing a lysing agent is contacted to a cell-containing suspension soas to effect lysing of the cells and the liberation of the cellularcontents for further analysis. As another example, a particle-bearingsurface where the particles include ligands specific to a particularbiological species is contacted to a biological sample that containsthat species. The surface then binds that species, immobilizing thespecies for further analysis.

As one example, a surface bearing particles that are complementary to aspecific species may also be used as a filter to remove that speciesfrom a given sample. This may be accomplished by, for example,configuring the particle-bearing surface as a filter or otherhigh-surface structure so as to afford the surface the maximalopportunity to contact the sample.

Methods for embedding particles are further disclosed. These methodsinclude applying to a substrate a population of particles to thesubstrate under such conditions that one or more of the particles is atleast partially embedded in the substrate, the population of particlescomprising an average characteristic dimension in the range of fromabout 0.1 nm to about 1 cm; suitable substrates and particles aredisclosed elsewhere herein.

Applying the particles is suitably accomplished by propelling, spraying,atomizing, dropping, nebulizing, pouring, dripping, and the like. In oneembodiment, the particles are propelled—by, e.g., a sprayer—into thesubstrate, where they are embedded by impact with the substrate.Particles may also, where suitable, be propelled by an electric field ora magnetic field or other gradient, as described elsewhere herein.

In some embodiments, the particles are disposed in a fluid, as describedelsewhere herein. The substrate may also be heated, the particles may beheated, or both.

The present invention also provides methods for distributing particlesacross a surface. These methods include dispersing a population ofparticles in a fluid inert to at least one substrate; and disposing thefluid across a surface of the at least one substrate.

The population of particles is suitably evenly dispersed within thefluid. This even disposition may be accomplished by sonicating thepopulation of particles; other methods for even distribution will beapparent to those of ordinary skill in the art. In some embodiments, thefluid, one or more particles, or both, include at least one agentcapable of at least partially inhibiting inter-particle agglomeration,as described elsewhere herein. In other embodiments, the dispersion ofthe particles is at least partly effected by application of a gradient;suitable gradients are described elsewhere herein.

The methods also include removal of at least a portion of the fluid.This is suitably performed so as to leave behind an essentially uniformdistribution of particles across the surface. Removal of the fluid maybe accomplished by evaporation, application of reduced pressure, and thelike.

ADDITIONAL NON-LIMITING EMBODIMENTS Imaging

The process as described in the present application is useful to enhanceany polymer containing object with high-contrast agents that canincrease the contrast/noise ratio in MRI, X-ray imaging, ComputedTomography (CT), ultrasound, or other imaging tools. The polymer to betreated can be a medical device, a material used during surgery, or anypolymer-containing object that may find its way into a body that needsto be imaged.

As one non-limiting example, after surgical intervention in livingorganisms, it is desirable to confirm that any foreign bodies or objectsnot intended to be left in the organism are accounted for. In spite ofmany precautions, foreign materials can be accidentally left in thebody, which can compromise patient health. While certain devices, suchas stitches and stents, are intended to be left in the body, thesedevices can be difficult to image. It is thus advantageous that objectsinvolved in a surgical intervention that contain polymeric materials,which tend to have a comparatively low contrast on X-rays, MRIs, orother imaging techniques, be treated with particles that provide highercontrast when viewed with X-rays or MRI or other such technique. Some ofthese materials and devices include medical devices, medical equipment,medical instruments, stitches, sponges, gauzes, gloves, safety goggles,clamps, and the like.

In typical medical settings, contrast media are used to enhance thevisibility of objects. As one example, a radio-opaque substance may beused during an x-ray to enhance the visibility of structures within thebody. For MRI imaging, the contrast agents alter the magnetic propertiesof nearby hydrogen nuclei; such contrast may be positive or negative.Positive contrast media have higher attenuation density than thesurrounding tissue—making the contrast look more opaque—while negativecontrast media has lower attenuation (i.e., makes the contrast look lessopaque). Negative contrast is typically found only as a gas.

The high-contrast agents can be particles as described above but willtypically contain elements that have high atomic numbers. Some examplesof these particles are: gold particles and nanoparticles, silverparticles, copper particles, platinum particles, titanium particles,iodine containing particles or compounds, barium-containing particles orcompounds, diatrizoate, metizoate, ioxaglatc, iopamidol, iohexyl,ioxilan, iopromide, iodixanol, and the like. Gadolinium-containingparticles or compounds can also be used as a component of MRI contrast.

Once the substrate of the material or device to be contrast-enhanced hasbeen identified, a suitable fluid is chosen as a softener for thesurface. As described elsewhere herein, there are a number of possiblesolvents or liquids and combinations thereof that can achieve thispurpose, and the optimal combination of materials and fluids will bedictated by the needs of the user. Subsequently, particles that havecharacteristically high-contrast will be added to the liquid, and willbe mixed to achieve some level of uniformity via physical agitation orby adding stabilizers, or by way of certain surface chemistries.

The resulting solution may then be applied to the substrate so as toembed the contrast-enhancing particles in the substrate. The particleswill then in turn cause the treated objects to more easily discerniblethrough the imaging and observational techniques referenced above.

Diagnostic Biosensor Applications

The claimed invention also enables diagnostic biosensors for thedetection of cancer, genetic disease, and other ailments. For example,to detect certain DNA, RNA, or other nucleic acid sequences, or todetect antigens and other biomolecules, complementary nucleic acidsequences or corresponding antibodies are localized on a polymersubstrate such that a positive match between a detector moiety and anantibody leads to a discernible change. For example, metallicnanoparticles such as gold nanoparticles may be embedded in a plasticsubstrate according to the claimed methods and single-stranded DNA orantibodies may be bound to the nanoparticles through a thiol group orother surface attachment methods. Particles may also be embedded withthe biomolecule binding sites already emplaced on the particles prior toembedding.

Following introduction of a solution, e.g., blood, enzyme digestedblood, other biofluid, to a plastic surface enhanced in this way, thetarget DNA, proteins, etc will bind to the nanoparticles. The presenceof the target molecules can be detected via a change in voltage, lightintensity, mass, or other discernible change, which change may beamplified or otherwise enhanced through the binding of additionalparticles or markers, e.g. fluorescing molecules, at the location of thebinding. Such a device may effect a visible change upon the binding oftarget compounds, making a separate reader unnecessary for the result ofthe test. Because the target molecules are bound to the particlesembedded in a surface, the bound molecule will likely resist beingdisplaced by moderate rinsing. If stronger methods—such as vigorousrinsing, heating, or the introduction of bond-cleaving agents—are used,the target molecules may be displaced, thus permitting re-use of thebiosensor.

Electronics Applications

As discussed elsewhere herein, carbon nanotubes, nanowires, andnanoparticles are some of the particle types that may be used for theproduction of wires, transistors, resistors, capacitors, memristors, andother components of electronic circuits or devices, such aslight-emitting diodes (LEDs) through this process, but any of theparticles described in this document are applicable.

As one non-limiting example, particles are embedded into the surface ofa thin layer of conducting polymer to tune the polymer's electronicproperties, e.g., to vary the type or degree of resisting, conducting,and semiconducting. In another example, metallic nanoparticles areembedded in the surface of a polymer to form a conducting path, due totouching or proximity of the particles to one other or due to a heating,reduction-oxidation reaction, or other process to fuse the particles.

As another example, to solve the problems of fluorescent lights burningout or of having a delay before they generate light after electricity isrun through them, carbon nanotubes or nanowires or other particles ofdisproportionate aspect ratio may be embedded into a conducting polymersubstrate such one end of the nanotube or nanowire is free of thesubstrate and capable of emitting electrons upon passage of a currentthrough the conducting polymer. Similarly, nanowires, nanotubes, orparticles having disproportionate aspect ratios—again with an unembeddedend—may be used as part of a field emission display (FED) or otherdisplay technology as a generator of electrons—such as a cathode—toenable the illumination of a pixel or other visible display entity bycausing a phosphor or other material to emit light. Wavelengths otherthan those of visible light may be produced as well.

Embedded particles—again with unembedded ends—may function as part of aprobe. This enables massively parallel reading and writing to a storagedevice or massively parallel AFM or other probe microscopy. Such treatedsurfaces are also useful as an interface with biological cells orneurons.

In the aforementioned examples involving nanowires, nanotubes, or otherparticles embedded in a surface but also having an unembedded end, analternate mechanism could be used to localize the nanowires or carbonnanotubes on the surface. Instead of directly embedding nanowires orcarbon nanotubes into the surface such that one end remains unembeddedin the surface, catalytic or reactive nanoparticles could be embedded inthe surface, which would then catalyze the growth of nanowires or carbonnanotubes at the regions where the nanoparticles had been embedded.

A current passed through the substrate or a field generated around thesurface then promotes nanowires or nanotubes having one end extendingaway from the surface during or after growth. In all of the aboveexamples involving nanowires or carbon nanotubes or other such particlesembedded in a conducting polymer surface with an unembedded end, thedevices may also function if the substrate is a nonconducting polymerlayer coated on top of a conducting substrate, where electrons traversethe nonconducting layer.

Antistatic Applications

Anti-static additives are used in many plastics to inhibit accumulationof electrical charge on the product surface. Because plastics aretypically inherently electrically insulating, they have a tendency toaccumulate such charge. Antistatic additives reduce and can eliminatethe gathering of dust and dirt, lowering the risk of sparks on productssuch as furniture and flooring, packaging, consumer electronics, andstationary. Without being bound to any single theory operation, it isbelieve that these additives function by lowering the overallresistivity of the treated article.

Instead of being incorporated into products through bulk incorporationor coating, as is currently done, plastic surfaces can be madeantistatic by incorporation of antistatic agents or particles by way ofthe claimed methods. Various antistatic additives are capable ofincorporation into the surface of plastics via the claimed processes;these antistatic particles can be anionic, cationic, non-ionic, orpolymeric in nature. The three principal chemistries of these antistaticagents are ethoxylated amine (EA), glycerol monostearate (GMS), andlauric diethanolamide (LDN), each of which is amenable to the disclosedmethods and compositions.

RFID (Radio-Frequency Identification) Tags

The process as described in this patent application can be used tocreate an RFID tag, in a number of different ways. These tags can alsobe used with frequencies that are not limited to radio frequencies, butcan be used with both higher and lower frequencies such as microwaves,infrared, x-rays, and other.

RFID tags normally contain two parts—an integrated circuit for storingand processing information, modulating, and demodulating an RF signal,and an antenna for receiving and transmitting the signal. There areactive, passive, and semi-passive RFID tags.

The process described in this patent application can be used to createthe antennae that are used to pick up a signal and re-transmit it. Theprocess as described when used in conjunction with conductive particlescan be used to create a conducting coil pathway that acts as an antenna.The antennae need not be coil-shaped, and need only be capable of havingelectrical current induced in the antenna by the incoming frequencysignal, or be capable of transmitting an outgoing signal, or both. Ifthe particles embedded in the surface are not touching or do nototherwise form a conducting pathway, the particles can be joined using anumber of different methods, including sintering the particles so thatthey fuse together, or applying a solution containing ions or particlesthat will deposit as metal onto the embedded particles to fuse particlesand form a conductive pathway.

One type of antenna created by the present invention is a magneticdipole antenna. The reader antenna can be a single coil that istypically forming a series or parallel resonant circuit, or a doubleloop—transformer—antenna coil.

Magnetic ID Applications

The process described in this patent application can be used to createunique magnetic identifications for the purposes of authentication ortracking. By using the process described in this patent application withmagnetic, paramagnetic, diamagnetic, ferromagnetic, antiferromagnetic,ferromagnetic, metamagnetic, superparamagnetic, and other types ofparticles, unique and non-replicable magnetic signatures are created.Because the particles embedded in such a process are oriented anddistributed randomly, each application will have a differentconfiguration.

At present, the traditional magnetic barcode of a credit card can bereplicated easily. Replication of a similar barcode made according tothe present invention would be more difficult, because the sheer numberof particles and the fine distribution of the particles renders theexact magnetic signature statistically less replicable. In otherembodiments, by inducing a magnetic field in the environment surroundingthe spray environment during spraying and until the surface hardens, acontrolled and replicable magnetic pattern may be achieved. Thus, theprocess described in this application is used to create both extremelyrandom or extremely ordered magnetic patterns on substrates.

Antimicrobial and Toxin-Neutralizing Applications

Polymer surfaces that interface with water, such as bottles, vessels,tanks, pipes, hydration bladders, valves and tubes of hydration packs,filters, valves, and spouts, may be treated by the process describedwith antimicrobial particles that will protect the surfaces, and alsotreat the water and deactivate microbial contaminants. Examples of suchparticles include ion-exchanged zeolites, silver-loaded insolublephosphates, silver-loaded calcium phosphate, silver-ion-modified glass,silver-ion-exchanged potassium titanate fiber, silver-loaded inorganiccolloid, silver nano or micro particles, and the same using copper,zinc, or other metallic ions, metallic nanoparticles, ion-loaded glass,ion-exchanged zirconium phosphate-based ceramics and other ceramics,zinc pyrithione particles, copper pyrithione particles, and the like.

The effect of silver nanoparticles is shown in FIG. 6. The left side ofthat figure depicts a population of E. coli bacteria. At the right ofFIG. 6 is the same population of bacteria after treatment withliquid-borne silver nanoparticles, which treatment caused the formationof pits—shown as blackened regions—on the bacteria, which increase thebacteria's permeability, which eventually leads to cell lysis.

Aside from embedding antimicrobial particles, other particles may beembedded to impart additional functionality. Particles for neutralizingknown toxins and other hazardous chemicals and substances may also beembedded. For example, iron oxide—rust—particles may be embedded todecrease arsenic content of the water interfacing with the surfacethrough adsorption. Iron nanoparticles may also be embedded and used todecrease the concentrations of chlorinated methanes, chlorinatedethenes, chlorinated ethanes, chlorinated benzenes, polychlorinatedbenzenes, lindane, Cr(VI), Pb(II), Ni(II), Cd(II), perchlorate.Single-wall carbon nanotubes (SWNTs), other sorts of nanotubes, andother carbon structures may be embedded to absorb dioxins and otherorganic compounds, and can even absorb bacteria and other organisms.Embedded carbon nanotubes could also absorb a variety of other compoundsincluding sodium chloride, sodium sulfate, calcium chloride, magnesiumsulfate, sulfuric acid, hydrochloric acid, fructose, sucrose, humicacid, viruses, proteins, and bacteria.

Common objects may also be embedded with antimicrobial-acting particles.A non-exclusive listing of such objects includes keyboards; computermouse; clear film with pressure sensitive adhesive backing; foodcontainers; water containers and bottles; eating and cooking utensils;shower curtains; water and beverage dispensers; shopping cart handlesand shopping carts; hydration packs, bladders, valves, tubing, and bags;water pipes; sewage pipes, gas pipes, footwear, cell phones; video gamecontrollers and buttons; laptop and ultraportable computers, mouse padsand pointing pads; vehicle steering wheels; vehicle plastic surfaces,vehicle buttons, vehicle vents, train and subway supports and handrails;airplane and train tray tables, armrests, windowshades, cutting boards;trash cans; dish drying rack and pan; fish tank tubing; fish tankfilters, lobster traps; fish nets and tanks; boat hulls; refrigeratorsealing gaskets; refrigerator surfaces; biometric readers such as fingerand palm print readers; boat and other water-based propellers;humidifier and dehumidifier tanks and surfaces; shower mat; gym and yogamat; gym equipment; catheters; intubation tubes; implantable devices andmaterials; newborn baby holders used at hospitals; premature infantholders; bathroom and shower soap and shampoo dispensers; plastichandles and knobs for doors, cabinets, sinks, showers and similar; ATMkeypads; ATM screens and screen protectors; credit cards and otherplastic cards; salt, pepper, and similar shakers; athletic helmet strapsand interior helmet padding; litter boxes; pet bowls for food and water;pet carriers; subway, train, car, restaurant, or other scats havingpolymer coverings; table surfaces and counter top surfaces andrefinishings; placemats; colanders; tanks; medical tool trays; plasticmedical tools, orthodontic devices, table tops, faceplates for consumerelectronics; remote controls; tiles, shower surfaces; toilet surfaces;trash bins and lids and handles. Other applications will be apparent tothose of ordinary skill in the art.

Catalytics

The process as described above is also applicable to creating catalyticsurfaces. The process described above can be with traditionalheterogeneous catalysts like vanadium oxide, nickel, alumina, platinum,rhodium, palladium, mesoporous silicates, etc. Similarly, somehomogeneous catalysts can be used like: enzymes, abzymes, ribozymes,deoxyribozymes, and the like. Electro-catalysts are also suitable,including, for example, platinum nanoparticles. Organocatalysts are alsosubstances that can suitably be embedded into a surface

Application of the claimed invention to catalytics is useful in growthof nanowires, nanorods, or nanotubes, where a gold, silver, or othermetallic particle or nanoparticle acts as the growth catalyst. As onenon-limiting example, gold nanoparticles may be embedded into substrateand used to grow nanowires, nanorods, or nanotubes, thereby producing astructure having these structures embedded within and projectingoutward.

Catalytic converters can also be made using the claimed invention. Thereare several components of the catalytic converter, the core, thewashcoat, and the catalyst itself. The washcoat is a rough surface thatincreases surface area, and the core is usually a high-surface areasupport for the catalysts. In standard catalytic converters, platinumand manganese are catalysts that help break down some of the moreharmful byproducts of automobile exhaust. The catalyst is normallyplatinum, but palladium and rhodium are also used. Cerium, iron,manganese, nickel, and copper may also be used. Other metals orcatalytic material could also be used. The process described above couldbe used to embed these catalysts into the core or other parts of thecatalytic converter.

Other potential uses would be in catalysis-based chemical productionprocesses like the Haber process, that is used to produce ammonia. Thismultiple step process uses multiple different types of catalysts. Forexample, nickel oxide is used during steam reforming, mixtures of iron,chromium, and copper, as well as copper, zinc, and aluminum, are alsoused during the process as catalysts for different parts of thereaction. In the final stage of the process, magnetite—iron oxide as thecatalyst—is used. Other catalysts could be used as well, by using theprocess described above to embed these catalytic particles into asurface.

This could also be used to create a pipe or container surface that canbe used to catalyze a gas or liquid reaction. The process could also beused to create a filter, where as a liquid or gas passes through thefilter it contacts the catalytic surface.

Fragrance and Flavor Applications

Products, packaging materials, and films may be enhanced with flavor andfragrance via the process described in this patent application.Compounds capable of providing flavor or fragrance can be incorporatedinto controlled-release particles may be compatible with the processdescribed in this application. Some applications for odor neturalizingand fragrances include trash bins and toilet seats.

The process as described above can also be used to enhance surfaces withflavors or scents. By using particles like silica shells, absorbentpolymer beads, buckyballs, nanotubes, or other encapsulation particles,certain flavors or scents can be captured. Using the process above, onecan embed the encapsulated flavors/scents into the surface of thingslike toys, novelty items, plastic spoons, forks, knives, straws, andother utensils, and dental retainers, pacifiers, animal toys, and thelike.

Antimicrobial Testing

The following are exemplary, non-limiting embodiments of the claimedinvention as applied to antimicrobial applications. These embodiments donot limit the scope of the claimed invention in any way and are forillustrative purposes.

1. Aerosol Treatment

The conditions of freshly extruded PVC pipe were simulated using anumber of methods including via fiber extruder and hot press. Silverpowder was then aerosolized onto the molten PVC surface to create auniform dispersion of particles on the surface. The aerosol generatorused was built by linking an air gun to a nanoparticles reservoir and toa thin pipette (which acted as the barrel) via a series of adapters.Bursts of air aerosolized the nanoparticles and pushed them through thepipette and towards the target.

1.1 Fiber Extruder

Using a fiber extruder (DACA Instruments' SpinLine Fiber Extruder),industrial-grade PVC pellets were extruded through a 1 mm diameteraperture. The PVC pellets were heated for 30 minutes to temperaturesranging from 150-185° C. and fibers were extruded at speeds ranging from1-20 mm/minute. Nanoparticles were aerosolized onto the hot extrudedsurface.

1.2 Hot Press

Flat industrial-grade PVC samples and freshly extruded PVC samples(fabricated using the fiber extruder, were placed between two steelplates that were heated to temperatures ranging from 150-185° C. andpressed at pressures ranging from 1,000-15,000 lbs. The PVC samples wereremoved at time periods ranging from 30 seconds to 30 minutes, and wereexamined Silver microparticles (Powder, 2.0-3.5 μm, 99+%. Sigma-Aldrich,www.sigma-aldrich.com, Cat. No. 327085) were then aerosolized onto theresulting hot and softened PVC surfaces.

2. Solvent Treatment Method

2.1 Substrate Preparation

Flat industrial-grade PVC sheets were used as the substrate fordepositing antimicrobial silver treatment. For all tests other than ASTME2180, these large sheets were cut into 1.2×1.2 cm pieces, using a PVCclamp-cutter (Home Depot, www.homedepot.com). For the purpose of theASTM E2180 test, PVC sample substrates were cut into 3×3 cm. All PVCsubstrate samples were washed with soap and water followed by methanoland ethanol.

2.2 Suspension of Silver Nanoparticles

Silver nanoparticles were suspended in tetrahydrofuran (THF), an organicsolvent. High molecular weight PVC powder (HMW PVC powder. Fluka<www.sigma-aldrich.com>, Cat. No. 81387) and silver nanopowder(Nanopowder, <100 nm, 99.5% (metals basis) (Sigma-Aldrichwww.sigma-aldrich.com, Cat. No. 576832) were added in various weightpercentages to THF. The resulting solutions were sonicated to aid thedissolution of the PVC powder and suspension of the silver particles;sonication of PVC in THF prior to addition of silver nanopowder resultedin better suspension formation. The efficacy of PVC powder as astabilizing agent was investigated by comparing plain silver suspensionsto PVC-stabilized silver suspensions. PVC concentrations were variedfrom 0.0 wt % to 3.0 wt % and silver concentrations were varied from0.45 wt % to 4.0 wt %.

2.3 Substrate Treatment

The application of silver nanoparticle solutions onto all PVC substrateswas accomplished using a spin-coater. The 1.2×1.2 cm samples werespin-coated at 1500 rpm for 33 seconds with 10 drops of silver solutionsequentially added immediately after spinning was initiated. The 3×3 cmsamples were spin-coated at 3000 rpm for 33 seconds with the equivalentof 10 drops squirted quickly onto the sample immediately after spinningwas initiated. The above values for spin-speed, number of drops, andmethod of applications were chosen after extensive trials for optimizingthe embedding of the silver particle as a function of these parameters.

2.4 Characterization Using Raman Spectroscopy

The silver nanoparticles and the surface of silver-treated PVC sampleswere characterized via Raman spectrometry (Renishaw RM1000 VIS RamanMicrospectrometer, Drexel University <www.nano.drexel.edu/Facilities).The silver-treated PVC samples were placed under the optical microscopeand were focused at 50× magnification. The optical portion of thespectrometer was then turned off and the green argon-ion laser (λ=514.5nm, 1% intensity to prevent sample burn) was focused on the samples. TheRaman scattering responses were then measured with 10 passes,approximately 10 seconds each pass, and were analyzed to determine thecomposition of the targeted area. All scattered intensity data wererecorded on a relative scale.

2.5 Characterization Using Optical Microscopy

Optical micrographs of silver-treated PVC surfaces and control sampleswere obtained and analyzed to characterize the silver treatment. Thesamples were placed under an optical microscope and focused at 20×magnification, which magnification level was chosen for its wider fieldof view and superior resolution. ImageJ software (ImageJ;http://rsb.info.nih.gov/ij/) was used to improve image characteristicsand measure particle dispersion characteristics, such as averageparticle size and the area fraction of particle coverage.

2.6 Characterization Using Scanning Electron Microscopy

Nanoscale surface characterization was achieved using the Focused IonBeam (FIB) SEM10 (FEI Strata DB235, www.fei.com). The silver-treated PVCsamples were first sputter-coated with gold palladium for 30 seconds at30 milliamps and then analyzed using the FIB. In addition to observingthe local structure of the silver particles on the sample surface, theFIB was used to cut through a silver particle and into the PVC surfaceto reveal a cross-sectional view of the embedded particle.

2.7 Durability Testing

Preliminary durability tests were undertaken to assess the effect ofcontinuous water flow over the silver-enhanced PVC surface. Four PVCsamples treated with a single silver solution (2 wt % silver and 2.25 wt% PVC powder) were fixed in place and subjected to a continuous streamof water having flow rate of 3.9 gal/min·in². This water flow wasproduced by altering the flow of water from a common tap using a plasticsheet. Recommended flow rates in commercial PVC pipes used for watertransportation were between 0.4 and 8.0 gal/min·in². The sample surfaceswere characterized using optical microscopy before the test and after2.5, 8, 26, and 51 hours. The area fraction of surface coverage of eachsample was determined using ImageJ routines.

2.8 Antibacterial Testing

To qualitatively and quantitatively characterize the antibacterialactivity of the nanoparticles and of the silver-enhanced samples, anumber of tests were used. Kirby-Bauer, Turbidity, Growth Analysis, andASTM E-2180 tests were conducted. Appropriate controls were used in alltests, and all samples were rinsed with ethanol before use.

2.8.1 Kirby-Bauer

Modified Kirby-Bauer tests were run to qualitatively verify the knownantibacterial properties of silver nanoparticles and to qualitativelyobserve the antibacterial properties of silver-enhanced samples.Sterile, 10 cm Luria-Burtani (LB) plates (1.0% Tryptone, 0.5% yeastextract, 1.0% NaCl, 1.5% agar, Teknova, www.teknova.com, Cat. No. L1100)were inoculated with Escherichia coli (Strain S., Fisher Scientfic,www.fishersci.com, Cat. No. S20918). To verify the antibacterialproperties of silver nanoparticles, a section of the agar surface wascovered in silver nanopowder using the aerosol generator discussed insection 2.1. To test the silver-enhanced PVC material, 1.2×1.2 cmsilver-enhanced PVC samples were placed coated side down onto the agar.Plates were incubated upside down in a lab oven at 37° C. for 24 hoursand zones of inhibition were measured when possible.

2.8.2 Turbidity

To qualitatively establish whether or not samples exhibitedantibacterial properties in aqueous solution, turbidity tests wereconducted. Sterile Luria-Burtani (LB) broth (received from theUniversity of Pennsylvania Department of Biology), was inoculated withEscherichia coli, and the resulting solution was placed in test tubes, 5ml per tube. 1.2×1.2 cm PVC samples were immediately immersed in thesolution in the tubes, one sample per test tube. Samples were incubatedwith loosened caps in a lab oven at 37° C. for 10 hrs and were observedfor turbidity via visual examination at hours 1, 2, 3, 4, 5, 6, 8, and10.

2.8.3 Growth Analysis

Antibacterial activity over time was assessed via growth analysistesting. The same initial procedure was used as for turbidity testing,as described elsewhere herein, but rather than perform visualobservations, 200 μl of solution was removed from each test tube andplated on LB plates (1.0% Tryptone, 0.5% yeast extract, 1.0% NaCl, 1.5%agar (Teknova www.teknova.com, Cat. No. L1100) at hours 1, 2, 3, 4, 5,6, 8, and 10. The plates were immediately refrigerated at 4° C. until 1hour after all plates were collected. The plates were then incubatedtogether in a lab oven at 37° C. and observed at hour 8. All sampleswere compared and a relative density scale was used, with 1 indicatinglowest bacteria growth and 10 indicating highest bacteria growth. ImageJwas used to quantify the bacteria density for plates where a full lawnhad not developed—all 4 wt % Ag 2.25 wt % plates—and that were notdestroyed due to application of bad dye (hour 3, 4, 5, 6, and 8). Thedye was intended to make the test results easier to analyze.

2.8.4 ASTM E2180

A FDA registered, independent microbiology laboratory (AccugenLaboratories, Inc. www.accugenlabs.com, Willowbrook, Ill.) wascontracted to perform a certified ASTM-E2180 test (ASTM Internationalwww.astm.org.), which was the Standard Test Method for Determining theActivity of Incorporated Antimicrobial Agent(s) In Polymeric orHydrophobic Materials. Staphylococcus aureus and Escherichia coli wereused as challenge organisms, Dey Engley (DE) neutralizing broth was usedas the neutralizer, contact time was 24 hours, and contact temperaturewas 35° C. Media and reagents used include soybean-casein digest agar,agar slurry, and sterile deionized water. A full protocol is availablefrom ASTM International.

3. Results

3.1 Aerosol Treatment Method

The aerosol treatment method was explored in an attempt to develop aprocess that could be integrated directly into the current manufacturingprocess for PVC pipes. The method, as described in section 2.1, involveda process by which particles could be aerosolized directly onto thesurface of freshly extruded pipes. Optical microscopy confirmed theadherence of silver particles to the surface of hot PVC, shown by FIG.7, but also indicated significant agglomeration of the silvernanoparticles. While research efforts for the aerosol treatment methoddisplayed promising results, the lack of access to an industrialtwin-screw extruder and guidance in industrial manufacturing processesfor PVC prevented further development of this method.

3.2 Solvent Treatment Method

3.2.1 Surface and Particle Analysis

3.2.1.1 Raman Spectroscopy

50% argon-ion laser intensity was used for the preliminary scans of purePVC and a strong Raman signal was recorded due to the highly reflectiveand white surface (FIG. 8). 1% light intensity was used for scans ofsilver-coated PVC samples (FIG. 8) in order to prevent burningassociated with the high absorbance of the dark colored silverparticles. This burning was later attributed to the burning off of theorganic coating on the silver nanoparticles. While Raman spectroscopywould not pick up a signal from pure silver, the molecular bondsassociated with the organic coating on the particles generated a Ramanscattering signal (FIG. 8). The Raman signal from the silver-treated PVCsubstrate closely matched the signal from the organically coated silvernanoparticles, confirming the presence of the silver nanoparticles onthe PVC surface. The peak in relative scattered intensity at ˜3000 cm⁻¹corresponded to a C—H bond and the peak at ˜1580 cm⁻¹ corresponded to aC—C bond. Because the Raman signal from the silver-treated PVC substratebarely matched the signal from untreated PVC, it could be concluded thatthe silver particles were exposed on the substrate surface and notcovered by PVC, thus allowing for the release of biocidal silver ions.

3.2.1.2 Optical Analysis

After confirming the identity of the particles on the surface of the PVCsamples, optical microscopy was used to study the characteristics of theparticulate dispersions (average particle size and area fraction ofsurface coverage) in order to optimize the embedding process. Averageparticle size and embedded area fraction values were significantlyinfluenced by the concentration of PVC powder and silver in the THFsolution. PVC powder was added to the solution in order to stabilize thesilver suspension (i.e. retard agglomeration over time) and encouragesmaller silver particles by increasing steric repulsion.

Silver particles in silver-THF solutions prepared without the additionof PVC visibly settled out faster than the silver particles inPVC-stabilized solutions, prepared with identical silver concentrations.Silver nanoparticles also agglomerated to a greater extent in silver-THFsolutions not stabilized with PVC. This greater agglomeration wasevident in the fact that average size of the silver particles on PVCsubstrates treated with unstabilized silver-THF solutions was larger(radius ˜6.3 μm for solution with 1.5 wt % silver and 0 wt % PVC) thanthe size of particles on substrates treated with stabilized solutions(radius ˜466.6 nm for solution with 1.5 wt % silver and 2.25 wt % PVC)(FIG. 9). As shown in FIG. 9, the average size of the silver particleson the PVC substrates also decreased with increasing PVC concentration,thus indicating that PVC retarded agglomeration and allowed for smallerparticle size. However, such a trend was not always achieved forincreasing PVC concentrations owing to various sources of error andpossibly complex relations between the concentration of silver and PVCadded to the silver-THF solutions.

Area fractions of the PVC samples embedded with silver strongly dependedon the concentration of silver in the silver-THF solutions. For constantconcentrations of PVC, the area fraction of surface coverage generallyincreased with increasing silver concentration (FIG. 10). Area fractionof surface coverage data corresponding to all PVC concentrationsexhibited a dip on increasing the silver concentration from 1.5 wt % to2.0 wt % (FIG. 10). Furthermore, the magnitude of this dip decreasedwith increasing PVC concentration. A possible explanation was that1.5-2.0 wt % silver represented some sort of agglomeration threshold andthat higher silver concentrations resulted in agglomeration, which inturn reduced the area fraction of surface coverage. Because higher PVCconcentrations prevented agglomeration to a greater degree, the decreasein area fraction of surface coverage became less significant withincreasing PVC concentration. However, the overall data set was noisydue to limitations in the image analysis software and several sources oferror discussed later.

As shown in FIG. 10, area fractions of surface coverage corresponding tosilver-THF solutions stabilized with higher concentrations of PVC powderwere in general higher than the area fractions of surface coveragecorresponding to solutions with lower PVC concentrations. Without beingbound to a single theory of operation, it is believed that this supportsthe theory that PVC powder helped stabilize the silver suspension andprevented agglomeration, thus leading to smaller and more finelydispersed silver particles on PVC substrates.

Average particle size also depended on silver concentration. FIG. 11demonstrates the following trend in average particle size: for lowvalues of silver concentration, average particle size increased slightlywith increasing silver concentration; at a critical agglomerationthreshold (1.5-2.0 wt % silver), average particle size increasedrapidly; for high values of silver concentration, average particle sizestabilized. Without being bound to any single theory of operation, it isbelieved that a given amount of stabilizer, 2.25 wt % PVC as in FIG. 11,can prevent agglomeration only up to certain silver concentrations,after which the stabilization effect—steric repulsion—was minimal andparticles agglomerated substantially. Depletion attraction and bridgingeffects may also explain the agglomeration.

Average particle size and area fraction of surface coverage data weresubject to severe limitation in the image analysis software and severalsources of error. While the Particle Analysis tool in ImageJ was veryaccurate, the process by which the optical images were converted tobinary black and white images for the purpose of analysis was subject toconsiderable human error. A substantial amount of human judgment wasused to adjust the gray-scale color used as a threshold to define theboundary of the silver particles such that the software picked up allthe smaller particles and large agglomerates, while eliminating unwantedreflections and light variations. While the area-fraction data was notaffected significantly by such judgment calls, the average particle sizedata was very strongly dependant on the threshold levels. Therefore theaverage particle size data could reflect significant inaccuracy. Thus,trends in average particle size were easier to interpret visuallythrough the optical micrographs (FIG. 9).

3.2.2 Durability Analysis

SEM images of a silver particle on the surface of PVC cut in half usinga FIB (FIG. 12) show that the particles are embedded into the PVCsubstrate. The small dots surrounding the silver particle in the figurerepresent the palladium gold coating, which was visible due to theburning of the underlying PVC substrate by the ion and electron beams.The features present in the wall of the trench cut by the FM wereunknown, but were also observed in the cross-section of an un-coated PVCsample (FIG. 12). Without being bound to any one theory, it is believedthat these features are stabilizers, such as aluminum, added toindustrial PVC to aid processing. Embedding the silver particles intothe PVC was the desired result of using THF as a dispersion medium sinceit was known to dissolve PVC in addition to most other plastics (ImageJ,http://rsb.info.nih.gov/ij/).

Embedding the silver particles allowed for a durable silver surfacetreatment that would resist erosion with continuous water flow. Thepreliminary durability test showed that the silver-coated area fractionof the PVC samples decreased over the first few hours of exposure towater flow but stabilized for up to 40 hours past this point, as shownin FIG. 13. The initial decrease could have been due to the erosion ofthe silver particles that were loosely embedded or not embedded into thePVC surface. Durability tests for longer timescales, for example timeperiods closer to the useful life of PVC pipe, remain to be conducted.

3.2.3 Antibacterial Analysis

3.2.3.1 Kirby-Bauer Test Results for Antimicrobial Properties of SilverNanoparticles

For experimental rigor, the antibacterial properties of the silvernanoparticles used for surface treatment in the current research werequalitatively verified. Modified Kirby-Bauer tests showed thatnanoparticle powder distributed across the surface of agar plates viaaerosolization inhibited the growth of Escherichia coli (FIG. 14). Dueto the distributed nature of the deposition technique, measuring zonesof inhibition was not possible. However, it is clear that the lawnformation that occurred in control samples without any silver particles(FIG. 14A, left plate) was inhibited by the presence of silvernanopowder on the surface of the agar (FIG. 14A, right plate).Increasing the amount of silver nanopowder spread across the surface ledto an increased antibacterial inhibition, to the point where no bacteriagrowth was observed.

3.2.3.2 Kirby-Bauer Test Results for Antimicrobial Properties of SilverNanoparticle Enhanced Polyvinyl Chloride

The Kirby-Bauer test is routinely used to observe the activity ofantibiotics. The test involves the placement of paper discs soaked inthe target antibiotic on the agar surface of bacteria growth plates. Theantibiotic diffuses into the agar, and inhibition of bacteria growth isobserved around the discs. The diameters of these zones of inhibitionare then measured and compared for determining relative antibioticeffectiveness. In the current study, silver-enhanced PVC samples wereplaced treated side down on inoculated agar plates; thus, diffusion ofsilver ions from the coating through the agar was the only theoreticalmechanism by which zones of inhibition could form.

FIG. 15A shows an uncoated control sample at the top of the figure, anda 2 wt % Ag 2.25 wt % PVC treated sample at the bottom of the figure, asviewed from the underside of a petri dish 24 hours after inoculationwith E. coli.

Results show the formation of a small zone of inhibition, about 0.88 mmwide at the maxima of the sides of the samples, FIG. 15B, in testsamples. The region of no growth was largest towards the center of thesides of the sample, consistent with the pattern expected if diffusionof ions occurred. Discoloration of the agar was not observed, whichsuggested that the zones of inhibition were not formed as a result ofdetachment of embedded silver particles. Thus, given the shape and colorof the zones of inhibition, ion diffusion is the suspected mechanism bywhich zones of inhibition formed.

3.2.3.3 Turbidity Test Results

Turbidity is directly related to the number of bacteria cells in a givensolution. By hour 4, the Control and 2 wt % Ag 2.25 wt % PVC samplesexhibited high turbidity relative to the 4 wt % Ag 2.25 wt % PVC samplesand to the sterile LB broth. The 4 wt % Ag 2.25 wt % PVC samplesexhibited similar translucence as the sterile LB broth. The samples wereobserved at hours 5, 6, 8, and 10 (FIG. 16), but no visible change inturbidity was observed for any samples. From these results, it appearsthat the treated PVC samples exhibit antibacterial activity, correlatedwith weight percent silver.

3.2.3.4 ASTM E2180 Results

The ASTM E2180 test is a standardized test, “designed to evaluate(quantitatively) the antimicrobial effectiveness of agents incorporatedor bound into or onto mainly flat (two dimensional) hydrophobic orpolymeric surfaces . . . . This method can confirm the presence ofantimicrobial activity in plastics or hydrophobic surfaces and allowsdetermination of quantitative differences in antimicrobial activitybetween untreated plastics or polymers and those with bound orincorporated low water-soluble antimicrobial agents” [1.0% Tryptone,0.5% yeast extract, 1.0% NaCl, 1.5% agar. Teknova, www.teknova.com, Cat.No. L1100]. An agar slurry was used to form a pseudo-biofilm on thesurface, reducing surface tension and providing more contact between theinoculum and the test surface. The ASTM E2180 results demonstrate a 100%reduction in the activity of all microorganisms within the first 24hours of exposure to the 4 wt % Ag 2.25 wt % PVC samples. BothGram-positive (S. aureus) and Gram-negative (E. coli) bacteria wereaffected. This conclusive and quantitative data is corroborated by thequalitative data collected via the modified Kirby-Bauer, Turbidity, andGrowth Analysis tests. Percent reduction in growth was obtained asfollows:

${\% \mspace{14mu} {Reduction}\mspace{14mu} {for}\mspace{14mu} {S.\mspace{11mu} {aureus}}} = {\frac{\left( {a - b} \right) \times 100}{a} = {\frac{\left( {{1.51 \times 10^{5}} - 0} \right) \times 100}{1.51 \times 10^{5}} = {100\%}}}$${\% \mspace{14mu} {Reduction}\mspace{14mu} {for}\mspace{14mu} {E.\mspace{11mu} {coli}}} = {\frac{\left( {a - b} \right) \times 100}{a} = {\frac{\left( {{5.13 \times 10^{5}} - 0} \right) \times 100}{5.13 \times 10^{5}} = {100\%}}}$

where, a=the antilog of the geometric mean of the number of organismsrecovered from the control samples after 24 hours and b=the antilog ofthe geometric mean of the number of organisms recovered from the treatedsamples after 24 hours.

Microorganisms recovered in 4 wt % Microorganisms recovered in Ag, 2.25wt % PVC sample after 24 Control sample after hours (cfu/ml) 24 hours(cfu/ml) Geom. Geom. Trial 1 Trial 2 Trial 3 Mean Trial 1 Trial 2 Trial3 Mean S. aureus <10 <10 <10 0 1.38 × 10⁵ 2.25 × 10⁵ 1.15 × 10⁵ 5.18 E.coli <10 <10 <10 0  4.6 × 10⁵  5.7 × 10⁵  5.1 × 10⁵ 5.71

Results show presence of antimicrobial activity (100% reduction for S.aureus, 100% reduction for E. coli).

4. Summary of PVC-Silver Results

Industrial-grade flat PVC sheets were embedded with silver particles andthe antibacterial properties of the resulting surface were confirmed.Silver nanopowder was suspended in THF and PVC solution and spin-coatedonto flat PVC substrates at concentrations of 0.45 wt % to 4.0 wt %. PVCpowder was used as a stabilizer at concentrations from 0.0 wt % to 3.0wt %. Raman spectroscopy confirmed the identity of the embeddedparticles as the organically coated silver nanoparticles. Opticalmicroscopy and ImageJ software were used to measure area fraction ofembedded surface coverage and average particle size for all samples.Embedded surface area fractions ranged from 0.1%-20% andparticle-agglomerate radii from 73 ran to 400 nm. Desired area fractionof embedded surface coverage and particle size dispersion werecontrolled by varying the concentration of silver and PVC powder in thesolution. Dissolving PVC powder in the silver solution helped stabilizethe suspension, retarding agglomeration.

Increasing PVC concentration, in general, led to smaller particle sizeand greater area fraction of embedded surface coverage. Increasingsilver concentrations, at constant PVC concentrations, resulted inhigher area fractions of embedded surface coverage and larger averageparticle size. Durability testing indicated that after an initial dropin area fraction, the embedded particles withstood continuous water-flowand remained securely embedded in the surface. SEM imaging confirmedthat the silver particles were embedded into the PVC substrate.

Antibacterial tests (Kirby-Bauer, Turbidity, and ASTM E2180) wereconducted using Gram-positive (Staphylococcus aureus) and Gram-negative(Escherichia coli) bacteria. Test results demonstrated the antibacterialproperties of silver treated samples. In particular, ASTM E2180 showedthat test samples coated with 4.0 wt % silver reduced S. aureus and E.coli activity by 100% within 24 hours. The treatment process developedin this research can be adapted for a variety of particles, substrates,and solvents. Thus, potential applications range from PVC pipes thatpurify water to materials that neutralize bio/chemical threats.

1-33. (canceled)
 34. A composite material, comprising: a substratehaving at least one surface in which a population of metallic nanowiresis at least partially embedded, the population of metallic nanowiresforming a conductive pathway by touching or proximity of the metallicnanowires to one another.
 35. The composite material of claim 34,wherein the substrate comprises a polymer. 36-39. (canceled)
 40. Thecomposite material of claim 35, wherein the polymer is characterized asconductive. 41-45. (canceled)
 46. The composite material of claim 34,wherein the population of metallic nanowires comprises silver. 47-64.(canceled)
 65. The composite material of claim 34, wherein the substrateis harder than the population of metallic nanowires. 66-122. (canceled)123. The composite material of claim 34, wherein the population ofmetallic nanowires provides a coverage of 10% or less of the surface ofthe substrate.
 124. The composite material of claim 34, wherein at leastone of the population of metallic nanowires is fully embedded below thesurface of the substrate.
 125. The composite material of claim 124,wherein at least another one of the population of metallic nanowiresincludes a first portion embedded below the surface of the substrate anda second portion exposed above the surface of the substrate.
 126. Thecomposite material of claim 34, wherein the population of metallicnanowires comprises metallic nanowires that are fused together.
 127. Thecomposite material of claim 34, wherein the population of metallicnanowires is localized in a surface portion of the substrate, such thata remaining portion of the substrate is devoid of any metallic nanowire.128. The composite material of claim 34, wherein the substrate is apolymeric sheet.
 129. The composite material of claim 34, wherein thesubstrate is a single-layer substrate.
 130. A display device comprisingthe composite material of claim
 34. 131. A composite material,comprising: a substrate having at least one surface in which nanowiresare at least partially embedded, the embedded nanowires are localized ina surface portion of the substrate, such that a remaining portion of thesubstrate is devoid of any nanowire, and the substrate, with theembedded nanowires, has a lower resistivity relative to the substrate inthe absence of the embedded nanowires.
 132. The composite material ofclaim 131, wherein the embedded nanowires comprise silver.
 133. Thecomposite material of claim 131, wherein at least one of the embeddednanowires is fully embedded below the surface of the substrate.
 134. Thecomposite material of claim 131, wherein at least one of the embeddednanowires includes a first portion embedded below the surface of thesubstrate and a second portion exposed above the surface of thesubstrate.
 135. The composite material of claim 131, wherein theembedded nanowires comprise nanowires that are fused together.
 136. Thecomposite material of claim 131, wherein the embedded nanowires form aconductive pathway by touching or proximity of the embedded nanowires toone another.
 137. The composite material of claim 131, wherein thesubstrate is an extruded polymeric substrate.
 138. The compositematerial of claim 131, wherein the substrate is a single-layersubstrate.
 139. A sensor device comprising the composite material ofclaim
 131. 140. A composite material, comprising: a substrate having atleast one surface in which a population of metallic particles is atleast partially embedded, the population of metallic particles forming aconductive pathway by touching or proximity of the metallic particles toone another.
 141. The composite material of claim 140, wherein thepopulation of metallic particles comprises nanowires, nanorods, or acombination thereof.
 142. The composite material of claim 140, whereinthe population of metallic particles comprises metallic particles ofdisproportionate aspect ratio.
 143. The composite material of claim 140,wherein the population of metallic particles comprises silver-containingparticles.
 144. The composite material of claim 140, wherein at leastone of the population of metallic particles is fully embedded below thesurface of the substrate.
 145. The composite material of claim 140,wherein at least one of the population of metallic particles ispartially exposed above the surface of the substrate.
 146. The compositematerial of claim 140, wherein the population of metallic particlescomprises metallic particles that are fused together.
 147. The compositematerial of claim 140, wherein the substrate is a single-layer,polymeric sheet.
 148. A display device comprising the composite materialof claim 140.